Join NDA and get the chance to work with some of the leading minds in regulatory affairs, pharmacovigilance, health technology assessment and scientific communications on a variety of projects, clients and geographies.

Who are we?

NDA Group is a world leading regulatory, drug development and medical device consultancy. Founded in Stockholm 24 years ago, by Lars-Helge Strömqvist we have grown from a small consultancy based in Upplands Väsby to an international company with offices in the UK, Germany, France, Switzerland and the US. However, our commitment to our work remains the same:

“We bring men, women and children, all over the world, the best possible medicines without unnecessary delay”

Over the years we have supported over 1 000 individual life science companies and work on a steady basis with over 400 different companies of all different sizes around the globe, from big pharma to small incubator biotechs just starting out on their drug development journey.

We act as a neutral and independent third party who understands the language and needs of both the industry and the regulators overseeing it. We bridge the communication gap between them. This is how we can make the regulatory process a ”win-win” situation, which in the end benefits the patient.

Our consultants all have different backgrounds. Some of us come from clinical research, others from regulatory affairs or may have been working for the agencies. Our unique NDA Advisory Board brings together some of the most prominent experts in regulatory affairs, pharmacovigilance and HTA. All are ex-regulators or senior industry leaders, renown for the contribution they have made to drug development throughout their careers.

Our broad experience is a good thing because it makes us stronger as a whole.

Learn more about our team

Why join NDA?

As a consultant joining NDA you will have the opportunity to work on a diverse and varied set of projects depending upon your own background and expertise area. We support clients through all phases of development and therapeutic areas. Have a look at our services to see examples of the breadth of work you could be involved in.

You will also have the opportunity to work alongside and learn from some of the most prominent experts in drug development whilst sharing your knowledge and experience with your colleagues. We believe in work/life balance and provide the flexibility to work from one of our offices* or from home depending on your needs and location. Whichever you choose your colleagues are always close by if you want to ask a question or bounce an idea.

(Current COVID guidelines are in place)

Voices from NDA

Lars- Helge Strömquist – Owner and Founder of NDA

“I wanted to create a company that reflected my own work ethic and values, a company that makes a difference and that secures that good medicines reach patients.”

Björn Carlsson – Advisory Board member – Nordics

“Coming from an agency, assessing work already done by someone else, it was refreshing to switch to be a part of and able to influence the development process. Here I can use my experience to advise on how to move a project forward in the best possible way, it is very rewarding.”

Finn Pulfer – Consultant – Germany

“My first contact with NDA was during my undergraduate studies when I did an intern project at the company. I discovered that here I could not only see the industry side but a get an outstanding overview of the entire process of drug development. The best part is that I learn so much. There is a constant challenge but always someone to go to for advice. We work together and learn from each other”


Privacy Notice For Candidates

As part of any recruitment activity, we collect and process Job Applicants’ personal data. At NDA we are committed to being transparent about how we collect and use your data whilst we meet our data protection obligations. Please read our Privacy Notice for Candidates for more information on how we handle your data.

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Your drug development needs are unique

Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.

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